adult product Recalls

989 recalls tagged with “adult product”.

Recalled Precaliber 20 Bicycle in Miami Green (MY 2024)
MEDIUM
CPSC

Trek and Electra Recall Bicycles With Coaster Brakes Over Crash Hazard (2025)

Trek and Electra recall certain bicycles and replacement rear wheels sold by Trek authorized retailers and Trek.com due to a crash hazard. The coaster brakes can fail to engage, increasing the risk of loss of rider control. Consumers should stop riding recalled bikes, check serial numbers starting with WTU located under the bottom bracket, and contact a Trek or Electra dealer to schedule a free, 3

Trek
The coaster
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Health & Personal Care
HIGH
FDA DRUG

Walgreens Saline Nasal Spray With Xylitol Recalled for Microbial Contamination (41,328 Bottles, 2025

Walgreens Saline Nasal Spray With Xylitol, distributed by Walgreens Co., is recalled nationwide. The product was found with microbial contamination, specifically Pseudomonas lactis, in a non-sterile formulation. Consumers should stop using the product immediately and contact Medical Products Laboratories, Inc. for guidance or consult a clinician.

Medical Products Laboratories
Microbial contamination
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Vehicles & Parts
HIGH
NHTSA

Nissan Kicks 2025 Recalled for Shift-to-Park Warning Failure

Nissan North America recalls 2025 Kicks vehicles due to a Shift-to-Park warning that may not activate when the vehicle is shut off in a gear other than Park. The recall targets 2025 Nissan Kicks. Nissan will reconfigure the BCM to activate the warning at no cost. Notifications began January 29, 2025, with more letters expected May 7, 2025.

Nissan
When the
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Vehicles & Parts
HIGH
NHTSA

Toyota recall affects 2023-2025 models, instrument cluster display may fail

Toyota Motor Engineering & Manufacturing recalls multiple 2023-2025 vehicles because the instrument panel may fail to display speed, braking and tire pressure alerts. Dealers will update software for non-PHEV models and inspect/possibly replace panels for PHEV models at no charge. Owner letters expected Oct 27, 2025. Contact Toyota at 1-800-331-4331; Lexus follow numbers 25LB05/25LA05.

Toyota
An instrument
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Food & Beverages
HIGH
FDA FOOD

Pacific Seafood Recalls 15,498 Lbs Raw Blackened Shrimp Peeled & Deveined Tail-Off Over Sulfite (202

Pacific Seafood recalled 15,498 pounds of Raw Blackened Shrimp Peeled & Deveined Tail-Off sold refrigerated after undeclared sulfite was detected. The product is a shrimp tray produced in Ecuador and distributed in Alabama, Florida and Massachusetts. Consumers should not eat the product and should contact Pacific Seafood Group for a refund or replacement.

Pacific Seafood
Undeclared Sulfite.
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Health & Personal Care
HIGH
FDA DRUG

Actavis Recalls Testosterone Gel Due to Leakage Risk

Actavis Laboratories recalled 15,944 cartons of Testosterone Gel on November 7, 2025. The recall follows a defect in the side-seal of the containers, which may allow product leakage. Consumers must stop using the product immediately and contact their healthcare providers for guidance.

TESTOSTERONE
Defective Container
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Health & Personal Care
HIGH
FDA DRUG

Fresenius Kabi Famotidine Injection Recall Expands for Microbial Contamination in 2.2 Million Vials

Fresenius Kabi USA, LLC recalls 2,199,850 vials of Famotidine Injection, U.S. distribution nationwide plus Alaska, Hawaii and Puerto Rico after endotoxin testing concerns. The microbial contamination risk prompted an immediate stop-use order. Healthcare providers and patients should follow recall guidance and seek alternatives through their providers.

Famotidine
Microbial Contamination
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Health & Personal Care
HIGH
FDA DEVICE

C.R. Bard Ureteral Stent Kit Recalled Due to Labeling Discrepancy

C.R. Bard recalled 116 units of its InLay Optima Ureteral Stent Kit on November 6, 2025. A labeling discrepancy may cause the actual size of the stent to differ from what is indicated on the label. The recall affects distribution across the U.S. and several countries worldwide.

C.R. Bard
Labeling discrepancy;
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Food & Beverages
HIGH
FDA FOOD

Laiwu Manhing Vegetables Fruits Co Onion Granules Recall for Foreign Objects (2025)

Laiwu Manhing Vegetables Fruits Co recalled 245 cartons of irradiated onion granules sold in California after foreign objects were found in the powder. The contamination is described as black plastic planting film. Consumers should not consume the product and should contact the company for refund or replacement via email.

Laiwu Manhing Vegetables Fruits Co
foreign objects
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Health & Personal Care
LOW
FDA DEVICE

GET TESTED INTERNATIONAL AB Female Fertility Test Recalled for Premarket Approval Violation (31Units

GET TESTED INTERNATIONAL AB recalled 31 Female Fertility Tests distributed nationwide in the US. The devices were distributed without premarket approval or clearance. Patients and healthcare providers should stop using the device immediately and contact GET TESTED INTERNATIONAL AB for instructions.

GET TESTED INTERNATIONAL AB
Distribution without
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Health & Personal Care
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB Heavy Metals Test Recall for 50 Units (2025)

GET TESTED INTERNATIONAL AB recalled 50 units of Heavy Metals Test distributed nationwide in the United States. The device was distributed without premarket FDA approval or clearance. Stop using the device immediately and contact GET TESTED INTERNATIONAL AB for instructions.

GET TESTED INTERNATIONAL AB
Distribution without
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Health & Personal Care
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB Food Sensitivity Test Large Recalled for 3 Units in 2025

GET TESTED INTERNATIONAL AB recalled 3 units of its Food Sensitivity Test Large sold nationwide in the United States. The device was distributed without FDA premarket approval or clearance. Consumers should stop using it and contact GET TESTED INTERNATIONAL AB or their healthcare provider for instructions.

GET TESTED INTERNATIONAL AB
Distribution without
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Health & Personal Care
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB PSA Test Recall 27 Units Distributed Nationwide 2025

GET TESTED INTERNATIONAL AB recalled 27 PSA Test devices distributed nationwide in the United States on 2025-11-03 after regulators found the device was distributed without premarket approval or clearance. The lack of PMA/clearance means the device did not receive required regulatory authorization before sale. Patients and healthcare providers should stop using the device immediately and follow 제조

GET TESTED INTERNATIONAL AB
Distribution without
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Health & Personal Care
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB D-Dimer Test Recall for 1,218 Units (2025)

GET TESTED INTERNATIONAL AB recalled 1,218 D-Dimer Test kits nationwide after distributing without premarket approval. The recall cites distribution without FDA premarket approval or clearance. Healthcare providers and patients should stop using the device immediately and follow all recall instructions.

GET TESTED INTERNATIONAL AB
Distribution without
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Tag Statistics

Total Recalls
989

Related Tags

vehicleoutdoorstop use immediatelyreplacement availablereturn for refundimmediate actionrepair availablebattery poweredmetalgaragekitchenelectrical hazard